EP0640601B1 - Benzamide derivative - Google Patents

Benzamide derivative Download PDF

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Publication number
EP0640601B1
EP0640601B1 EP92904979A EP92904979A EP0640601B1 EP 0640601 B1 EP0640601 B1 EP 0640601B1 EP 92904979 A EP92904979 A EP 92904979A EP 92904979 A EP92904979 A EP 92904979A EP 0640601 B1 EP0640601 B1 EP 0640601B1
Authority
EP
European Patent Office
Prior art keywords
chloro
methoxybenzamido
amino
azabicyclo
endo
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP92904979A
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German (de)
English (en)
French (fr)
Other versions
EP0640601A4 (en
EP0640601A1 (en
Inventor
Yasuo Ito
Hideo Kato
Shingo Yasuda
Nobuhiko Iwasaki
Hiroyuki Nishino
Makoto Takeshita
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Abbott Japan Co Ltd
Original Assignee
Hokuriku Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hokuriku Pharmaceutical Co Ltd filed Critical Hokuriku Pharmaceutical Co Ltd
Publication of EP0640601A4 publication Critical patent/EP0640601A4/en
Publication of EP0640601A1 publication Critical patent/EP0640601A1/en
Application granted granted Critical
Publication of EP0640601B1 publication Critical patent/EP0640601B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
    • C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/14—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing 9-azabicyclo [3.3.1] nonane ring systems, e.g. granatane, 2-aza-adamantane; Cyclic acetals thereof

Definitions

  • the present invention relates to novel benzamide derivatives which have excellent gastrointestinal stimulating activity and antiemetic activity and are useful as medicament for the treatment of gastrointestinal diseases.
  • the present invention further relates to a method for preparing said benzamide derivatives and a pharmaceutical composition useful for the treatment of gastrointestinal diseases comprising said benzamide derivative as an active ingredient.
  • Metoclopramide (The Merck Index, 11th Edition, 6063) as an antiemetic agent and a gastrointestinal prokinetic agent
  • various substituted benzamide derivatives having antiemetic activity and gastrointestinal stimulating activity have been provided.
  • the Merck Index (11th edition, 2344) discloses Clebopride which is a benzamide derivative having a piperidine ring and is useful as antiulcer agent.
  • the Merck Index (11th edition, 2318) discloses Cisapride useful as a gastrointestinal prokinetic agent. These drugs are widely used clinically.
  • Japanese Patent Unexamined Publication No. (Sho)55-92384 discloses that benzamide derivatives substituted with an azabicyclo ring have antiemetic activity and gastrointestinal stimulating activity and that they are useful as an antiemetic agent and a gastrointestinal prokinetic agent.
  • Document D3 discloses benzamides which have anti-depressant and/or anxiolytic activity, a process for their preparation and their use in the treatment of mammals.
  • substituted benzamide derivatives are not sufficiently useful since they do not have stimulating activity on lower digestive tracts such as the large intestine, although they have stimulating activity on upper digestive tracts such as the stomach. Furthermore, these substituted benzamide derivatives are not satisfactory from a safe standpoint since they sometimes cause adverse reactions such as extrapyramidal syndrome or hyperprolactinemia.
  • an object of the present invention is to provide medicament for the treatment of gastrointestinal diseases having stimulating activity not only on upper digestive tract but on lower digestive tract and reduced side effects.
  • novel benzamide derivatives of the present invention have stimulating activity both on upper digestive tract and lower digestive tract.
  • novel benzamide derivatives have reduced side effects and are useful as medicament for the treatment of gastrointestinal diseases having excellent selectivity.
  • the present invention was achieved on the basis of these findings.
  • the present invention provides benzamide derivatives represented by the following formula (I): wherein, R 1 represents a hydrogen atom or a C 1 -C 4 alkanoyl group; R 2 represents a hydrogen atom or a halogen atom; R 3 represents a C 1 -C 4 alkoxy group; R 4 represents a hydrogen atom or a C 1 -C 4 alkyl group; R 5 represents a hydrogen atom, a C 1 -C 4 alkyl group, or a C 1 -C 4 alkoxy group; A represents C 1 -C 7 alkylene group which may optionally be substituted with a C 1 -C 4 alkyl group; X represents a methylene group, an oxygen atom, or a sulfur atom; m represents an integer of from 0 to 3; n represents an integer of from 0 to 3; and p represents an integer of from 0 to 2, or pharmacologically acceptable salts thereof.
  • the benzamide derivatives are useful since they have gastrointestinal stimulating
  • a method for preparing said benzamide derivatives is provided.
  • a pharmaceutical composition useful for the treatment of gastrointestinal diseases which comprises said benzamide derivative as an active ingredient.
  • the pharmaceutical composition is useful as, for example, a gastrointestinal prokinetic agent, an antiemetic agent, an agent for the treatment of irritable bowel syndrome, and agent for the treatment of constipation.
  • a C 1 -C 4 alkanoyl group represented by R 1 may be, for example, formyl group, acetyl group, propanoyl group, butyroyl group, or trimethylacetyl group.
  • a halogen atom represented by R 2 may be, for example, a fluorine atom, a chlorine atom, or a bromine atom.
  • a C 1 -C 4 alkoxy group represented by R 3 and R 5 may be, for example, methoxy group, ethoxy group, propoxy group, isopropoxy group, butoxy group, isobutoxy group, or tert-butoxy group.
  • a C 1 -C 4 alkyl group represented by R 4 and R 5 or a C 1 -C 4 alkyl group which may optionally substitute on the alkylene group represented by A may be, for example, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, or tert-butyl group.
  • R 5 and Ph-CONH(CH 2 ) n - (wherein Ph represents a substituted phenyl) may substitute at any position of a ring comprising X and N.
  • Examples of pharmacologically acceptable salts of the benzamide drivatives of the present invention include alkali-addition salts or acid-addition salts.
  • alkali-addition salts include, for example, inorganic alkali-addition salts such as, for example, sodium salt, potassium salt, calcium salt, and ammonium salt, and organic base-addition salts such as, for example, ethylenediamine salt, ethanolamine salt, N,N-dialkylethanolamine salt, and triethanolamine salt.
  • acid addition salts include, for example, inorganic acid-addition salts such as, for example, hydrochloride, hydrobromide, hydroiodide, sulfate, nitrate, and phosphate, and organic acid-addition salts such as, for example, acetate, maleate, fumarate, citrate, oxalate, tartrate, malate, mandelate, methanesulfonate, p-toluenesulfonate, and 10-camphorsulfonate.
  • inorganic acid-addition salts such as, for example, hydrochloride, hydrobromide, hydroiodide, sulfate, nitrate, and phosphate
  • organic acid-addition salts such as, for example, acetate, maleate, fumarate, citrate, oxalate, tartrate, malate, mandelate, methanesulfonate, p-toluenesulfonate, and
  • the benzamide derivatives of the present invention represented by the above-described formula (I) may optionally have an asymmetric carbon atom.
  • Each of enantio-isomers distinguished by the asymmetric carbon atom, an arbitrary mixture thereof, and racemate, i.e., equimolor mixture thereof, fall within the scope of the present invention.
  • the benzamide derivatives of the present invention have more than one asymmetric carbon atoms, each diastereomer and an arbitrary mixture of the diastereomers also fall within the scope of the present invention.
  • the benzamide derivatives of the present invention may be in any one of possible conformations.
  • the compounds of the aforementioned formula (I) wherein p is 1, piperidine, morphorine, or thiamorphorine ring substituted with Ph-CONH(CB 2 ) n - group may be in any one of configurations selected from chair form, boat form, or twist-boat form.
  • compounds having Ph-CONH(CH 2 ) n - group and -(CH 2 ) m - cross linking group above the same side of a ring plane comprising X and N are referred to as endo-compounds, and compounds having each of the groups above the opposite sides of the plane are referred to as exo-compounds.
  • the benzamide derivative represented by formula (I) can be prepared according to a method described below which is an embodiment of the present invention. However, methods for preparing said compound are not limited to these processes.
  • a process for preparing the benzamide derivatives of the present invention represented by formula (I) comprises the following steps:
  • organic solvent used for the N-alkylation in the method of the present invention examples include, for example, alcohols such as, for example, methanol, ethanol, n-propanol, isopropanol, and n-butanol; aromatic hydrocarbons such as, for example, benzene, toluene, and xylene; and aprotic polar solvents such as, for example, tetrahydrofuran, 1,4-dioxane, acetonitrile, N,N-dimethylformamide, N-methyl-2-pyrrolidone, and dimethyl sulfoxide.
  • alcohols such as, for example, methanol, ethanol, n-propanol, isopropanol, and n-butanol
  • aromatic hydrocarbons such as, for example, benzene, toluene, and xylene
  • aprotic polar solvents such as, for example, tetrahydrofuran, 1,
  • Examples of the base used include, for example, metallic sodium, sodium hydride, sodium methoxide, sodium ethoxide, sodium amide, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium hydrogen carbonate, and potassium hydrogen carbonate.
  • the reaction may be carried out at from ice-cooling temperature to refluxing temperature of a solvent.
  • Halogenation may be carried out by the treatment with a halogenating agent in an organic solvent.
  • a halogenating agent used include, for example, chlorine, bromine, and sulfuryl chloride.
  • the organic solvent used include, for example, alcohols such as, for example, methanol, ethanol, and n-propanol; halogenated hydrocarbons such as, for example, dichloromethane, chloroform, carbon tetrachloride, and 1,2-dichloroethane; and aliphatic acids such as, for example, acetic acid.
  • the reaction may be carried out at from -30°C to refluxing temperature of a solvent.
  • Hydrolysis may be carried out by using an acid or a base.
  • acids such as hydrochloric acid or sulfric acid may be used
  • bases such as sodium hydroxide, potassium hydroxide, sodium carbonate, or potassium carbonate may be used.
  • These acids and bases may be used in the reaction in a form of aqueous solution, or alternatively, solutions in methanol, ethanol, n-propanol, isopropanol, n-butanol, sec-butanol, or tert-butanol, or solutions in aqueous organic solvents.
  • the reaction may be carried out at from ice-cooling temperature to refluxing temperature of a solvent.
  • the compounds represented by formula (II) used as starting materials in the aforementioned preparation process of the present invention are novel compounds with a few exceptions.
  • the compounds can be prepared according to the scheme set out below, in which R 1 , R 2 , R 3 , R 5 , X, m, n, and p are the same as those defined above, R 7 represents a C 1 -C 4 alkyl group, and Z represents a halogen atom.
  • Specific examples of the preparation process are given as reference examples in Examples which follows.
  • the benzamide derivatives represented by formula (I) prepared according to the process described above and their pharmacologically acceptable salts have hyderfunctional activity on digestive tract and are useful for the treatment of gastrointestinal diseases.
  • the compounds may preferably be formulated in a pharmaceutical composition as an active ingredient.
  • the pharmaceutical composition comprising said compound as an active ingredient may generally be formulated and administered to a patient as orally available compositions such as, for example, capsules, tablets, subtilized granules, granules, powder or syrup, or administered as injection, suppository, eye drop, eye ointment, ear drop, or topical composition.
  • compositions can be prepared by ordinary methods. If necessary, pharmacologically and pharmaceutically acceptable additives may be added.
  • excipients such as, for example, lactose, D-mannitol, cornstarch, or crystalline cellulose; disintegrants such as, for example, carboxymethylcellulose or calcium carboxymethylcellulose; binders such as, for example, hydroxypropylcellulose, hydroxypropylmethylcellulose, or polyvinylpyrrolidone; lubricants such as, for example, magnesium stearate or talc; coating agents such as, for example, hydroxypropylmethylcellulose, sucrose, or titanium oxide; or bases such as, for example polyethylene glycol or hard fat may be used as pharmaceutical additives.
  • solubilizing agents or solubilizers such as, for example, distilled water for injection, saline, or propylene glycol which is useful for an aqueous composition or a composition for preparing aqueous solution before use; pH adjusting agents such as, for example, an inorganic or organic acid or base; isotonicity agents such as, for example, sodium chloride, glucose, or glycerin; or stabilizers may be used as pharmaceutical additives.
  • suitable pharmaceutical additives ordinarily formulated in ointment, cream, or cataplasms such as white vaseline, macrogol, glycerin, or cloth may be used.
  • compositions of the present invention may be administered orally to an adult patient at a daily dose of about 0.1 to 500 mg.
  • the dose may be increased or decreased depending on the age or conditions of a patient.
  • Example 23 1 133.5 133.3
  • Example 24 0.1 116.0 134.8
  • Example 25 1 180.9 132.7
  • Example 27 0.1 113.4 134.5
  • Example 28 1 141.5 163.7
  • Example 32 1 176.7 158.5
  • Example 33 1 147.1 117.4
  • Example 34 1 187.0 191.5
  • Example 35 1 186.8 135.8
  • Example 36 1 195.9 119.6
  • Example 38 1 145.6 140.3
  • Example 39 0.1 134.7 159.1
  • Example 41 1 118.3 172.0
  • Example 43 1 166.5 504.8
  • Example 46 1 182.5 165.6
  • Example 58 0.1 180.7 217.5
  • Example 63 1 129.6 156.6
  • Example 64 0.1 200.3 234.5
  • Example 17 Ethyl endo-3-[3-(4-acetylamino-5-chloro-2-methoxybenzamido)-9-azabicyclo[3.3.1]non-9-yl]propionate sesquifumarate
  • Example 52 Ethyl cis-[4-(4-amino-5-chloro-2-methoxybenzamido)-3-methoxypiperidino]acetate hydrochloride
  • Example 54 Ethyl cis-6-[4-(4-amino-5-chloro-2-methoxybenzamido)-3-methoxypiperidino]hexanoate hydrochloride
  • Example 58 In the same manner as Example 58, the compounds of Examples 59-68 were obtained.
  • Example 65 cis-4-[4-(4-Amino-5-chloro-2-methoxybenzamido)-3-methoxypiperidino]butyric acid hydrochloride
  • Example 66 cis-6-[4-(4-Amino-5-chloro-2-methoxybenzamido)-3-methoxypiperidino]hexanoic acid hydrochloride
  • novel benzamide derivatives of the present invention represented by formula (I) have excellent gastrointestinal stimulating activity and antiemetic activity and thus are useful for the treatment of gastrointestinal diseases.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Hydrogenated Pyridines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
EP92904979A 1991-02-15 1992-02-12 Benzamide derivative Expired - Lifetime EP0640601B1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP4242591 1991-02-15
JP42425/91 1991-02-15
JP23375691 1991-08-22
JP233756/91 1991-08-22
PCT/JP1992/000134 WO1992014705A1 (fr) 1991-02-15 1992-02-12 Derive de benzamide

Publications (3)

Publication Number Publication Date
EP0640601A4 EP0640601A4 (en) 1994-03-07
EP0640601A1 EP0640601A1 (en) 1995-03-01
EP0640601B1 true EP0640601B1 (en) 1996-12-04

Family

ID=26382109

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92904979A Expired - Lifetime EP0640601B1 (en) 1991-02-15 1992-02-12 Benzamide derivative

Country Status (9)

Country Link
EP (1) EP0640601B1 (ko)
KR (1) KR0159961B1 (ko)
AT (1) ATE145906T1 (ko)
CA (1) CA2103590C (ko)
DE (1) DE69215694T2 (ko)
DK (1) DK0640601T3 (ko)
ES (1) ES2096073T3 (ko)
TW (2) TW213460B (ko)
WO (1) WO1992014705A1 (ko)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6750238B1 (en) 2000-05-12 2004-06-15 The University Of Toledo Aralkyl ester soft drugs
US7049326B2 (en) 2000-05-12 2006-05-23 The University Of Toledo Method and compositions for temporarily incapacitating subjects
USRE42412E1 (en) 2000-06-07 2011-05-31 Aryx Therapeutics, Inc. Materials and methods for the treatment of gastroesophageal reflux disease

Families Citing this family (17)

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CA2186623A1 (en) * 1994-03-30 1995-10-21 Takeshi Kawakita Benzoic acid compound and use thereof as medicine
US5686441A (en) * 1995-08-04 1997-11-11 Syphar Laboratories, Inc. Penam sulfones as β-lactamase inhibitors
EP0873990A1 (en) * 1995-09-22 1998-10-28 Yoshitomi Pharmaceutical Industries, Ltd. Benzoic acid compounds and medicinal use thereof
JP3529102B2 (ja) * 1997-07-11 2004-05-24 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノート シヤツプ ５−ｈｔ３および５−ｈｔ４介在性障害に有用な（＋）−ノルシサプリド
TW402591B (en) * 1997-07-11 2000-08-21 Janssen Pharmaceutica Nv Monocyclic benzamides of 3- or 4-substituted 4-(aminomethyl)-piperidine derivatives
AR022338A1 (es) 1999-02-04 2002-09-04 Hokuriku Pharmaceutical Un compuesto de benzamida, medicamento que lo contiene, y uso para la manufactura de un medicamento para el tratamiento o prevencion de una enfermedad digestiva o para mejorar la movilidad del tracto gastrointestinal.
AU2006201053B2 (en) * 2000-06-07 2008-01-31 Aryx Therapeutics Materials and methods for the treatment of gastroesophageal reflux disease
HUP0201980A3 (en) * 2002-06-13 2008-06-30 Richter Gedeon Nyrt Process for preparing a benzamide derivative and intermediates thereof
JP2006526000A (ja) * 2003-05-30 2006-11-16 ニューロームド テクノロジーズ、インク． Ｎ型カルシウムチャネル遮断薬としての３−アミノメチル−ピロリジン
WO2005068461A1 (en) 2004-01-07 2005-07-28 Aryx Therapeutics Stereoisomeric compounds and methods for the treatment of gastrointestinal and central nervous system disorders
US8138204B2 (en) 2004-01-07 2012-03-20 Aryx Therapeutics, Inc. Stereoisomeric compounds and methods for the treatment of gastrointestinal and central nervous system disorders
US8524736B2 (en) 2004-01-07 2013-09-03 Armetheon, Inc. Stereoisomeric compounds and methods for the treatment of gastrointestinal and central nervous system disorders
CA2620379C (en) 2005-08-31 2015-02-24 Aryx Therapeutics, Inc. Synthetic methods and intermediates for stereoisomeric compounds useful for the treatment of gastrointestinal and central nervous system disorders
KR100976063B1 (ko) * 2007-03-16 2010-08-17 동아제약주식회사 신규한 벤즈아미드 유도체 화합물 및 그의 제조방법
CN101402633A (zh) * 2007-09-11 2009-04-08 上海恒瑞医药有限公司 苯甲酰胺类衍生物、其制备方法及其在医药上的用途
TWI423967B (zh) 2008-02-21 2014-01-21 Dainippon Sumitomo Pharma Co 醯胺衍生物及含有其之醫藥組合物
US10570127B1 (en) 2018-11-05 2020-02-25 Renexxion, Llc Material and methods for the treatment of gastro-intestinal disorders

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GB1513631A (en) * 1976-02-17 1978-06-07 Gallardo Antonio Sa Piperidine derivatives
JPS5832878A (ja) * 1981-06-17 1983-02-25 ビ−チヤム・グレ−プ・ピ−エルシ− アルキルチオ誘導体、その製造法及びそれを含む医薬組成物
EP0099194A3 (en) * 1982-07-03 1984-04-11 Beecham Group Plc Novel benzamides
ZA854790B (en) * 1984-06-28 1986-02-26 Bristol Myers Co Pharmacologically active substituted benzamides
GB8527052D0 (en) * 1985-11-02 1985-12-04 Beecham Group Plc Compounds
US4870074A (en) * 1986-04-30 1989-09-26 Dainippon Pharmaceutical Co., Ltd. Substituted benzamide derivatives, for enhancing gastrointestinal motility
GB8718345D0 (en) * 1987-08-03 1987-09-09 Fordonal Sa N-substituted benzamides

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6750238B1 (en) 2000-05-12 2004-06-15 The University Of Toledo Aralkyl ester soft drugs
US7049326B2 (en) 2000-05-12 2006-05-23 The University Of Toledo Method and compositions for temporarily incapacitating subjects
US7164027B2 (en) 2000-05-12 2007-01-16 The University Of Toledo Aralkyl ester soft drugs
USRE42412E1 (en) 2000-06-07 2011-05-31 Aryx Therapeutics, Inc. Materials and methods for the treatment of gastroesophageal reflux disease

Also Published As

Publication number Publication date
WO1992014705A1 (fr) 1992-09-03
TW213460B (ko) 1993-09-21
ES2096073T3 (es) 1997-03-01
EP0640601A4 (en) 1994-03-07
ATE145906T1 (de) 1996-12-15
DK0640601T3 (da) 1997-06-02
EP0640601A1 (en) 1995-03-01
KR0159961B1 (ko) 1998-12-01
CA2103590A1 (en) 1992-08-16
TW243449B (ko) 1995-03-21
CA2103590C (en) 1999-06-01
DE69215694D1 (de) 1997-01-16
DE69215694T2 (de) 1997-05-28

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